Saturday, August 13, 2022

When the biodefense experts at Johns Hopkins warn you off ACAM-2000 vaccine for monkeypox, you know it is a really BAD vaccine

When the Johns Hopkins brain trust that lives off the fear of pandemics and biowarfare publishes an Op-Ed calling a TIME-OUT for the use of ACAM-2000 for monkeypox, you know this is a very bad, terrible vaccine. They are scared it will be the coup de grace that ends the vaccine enterprise as we know it.  And they are scared it could end their cozy sinecure as biodefense experts as well, after the COVID disaster brought about by experts. 

All the facts are not correct in the article below, though I cannot imagine why these biowarfare experts would make such obvious mistakes.  Maybe because CDC has also been very cagey about how much of these vaccines we have, and CDC butters JHU's bread.

The USG bought 300 million doses of ACAM2000 after 9/11, and more since.  The WaPo did an investigation in 2021 and revealed that once the anthrax vaccine manufacturer, Emergent BioSolutions bought the vaccine from Sanofi, the Assistant Secretary for Preparedness and Emergency Response, Robert Kadlec, ordered double the number of doses, and more than doubled the per-dose price.  And now the USG is looking for an excuse to offload some of this dangerous product.

After Robert Kadlec was confirmed as President Trump’s top official for public health preparedness in 2017, he began pressing to increase government stocks of a smallpox vaccine. His office ultimately made a deal to buy up to $2.8 billion of the vaccine from a company that once paid Kadlec as a consultant, a connection he did not disclose on a Senate questionnaire when he was nominated.

Under the agreement struck last year with Emergent BioSolutions, Kadlec’s office at the Department of Health and Human Services is paying more than double the price per dose it had previously paid for the drug. Because Emergent is the only licensed maker of the vaccine, Kadlec’s office arrived at the price through negotiations with the company rather than through bidding.

The Johns Hopkins authors are also cagey about the supposed shortage of Jynneos vaccine, the only smallpox vaccine that is also licensed for monkeypox.  As I have previously explained, the US government owns 16 million doses, sitting frozen in bulk storage in Denmark, purchased for a potential smallpox epidemic. Many more doses than this (20 million more?) were purchased since 2003 and have expired...but the USG has used expired vaccine before in an emergency.  If this monkeypox outbreak was a smallpox outbreak, how long do you think it would take before those doses got defrosted and bottled?  

The USG also expects delivery in 2022 and 2023 of 7 million more doses.

The supposed shortage is a scam.  And it now appears the scam is intended not only to turn a licensed vaccine (Jynneos) into a diluted EUA product, but also to push out some of the ACAM-2000 vaccine, which in my opinion is fit for only one thing:  incineration and license revocation.

https://www.statnews.com/2022/08/11/acam2000-full-fda-review-before-widespread-use-against-monkeypox/

 FIRST OPINION

As the United States grapples with monkeypox, which has been declared a public health emergency, one of the key strategies that will be used to control its spread is vaccinating high-risk individuals.

Demand for monkeypox vaccine far exceeds the supply.

When the outbreak began, the U.S. Strategic National Stockpile held a small supply of Jynneos, a vaccine licensed for monkeypox. The federal Administration for Strategic Preparedness and Response has allocated more than 1 million doses of Jynneos to state and local jurisdictions, yet full coverage of those at highest risk would require an estimated 3.2 million doses. Bavarian Nordic, the company that makes Jynneos, isn’t expected to be able to manufacture additional doses in the near term.

As the Washington Post has reported, the shortfall has increased external pressure on the Biden administration to turn to another vaccine, ACAM2000, to close the gap.

The Food and Drug Administration licensed ACAM2000 in 2007 to immunize people at high risk of smallpox infection. There is moderate evidence the vaccine will also work against monkeypox, which is closely related to smallpox.

More than 100 million doses of ACAM2000 were added to the Strategic National Stockpile in the years after the Sept. 11 and anthrax attacks as a hedge against the return of smallpox. Unlike Jynneos, which is not capable of replicating in the human body, ACAM2000 contains live, replication-competent vaccinia virus. Vaccinia is a pox family virus related to smallpox that cannot cause smallpox and leads to milder disease.

If the vaccination site is not cared for properly for the two to six weeks it takes to heal, the vaccinia virus can spread to other parts of the body, including the eyes and genitals.

It is not just the vaccine recipient who is at risk after ACAM2000 inoculation. Household members and others who come into close contact with the recipient are also at risk of developing vaccinia infection. This has special relevance to the current outbreak.

Gay, bisexual, and other men who have sex with men are currently at highest risk of monkeypox infection. They are also disproportionately affected by HIV, which can compromise the immune system if not properly treated. Although it seems unlikely that people living with HIV would be offered ACAM2000 because of the risk of adverse events, vaccinia transmission from a vaccinated person to someone with a compromised immune system is a serious risk. Other risks of ACAM2000 include myocarditis (inflammation of the heart muscle) or pericarditis (inflammation of the sac surrounding the heart), which occur in about 1 in every 175 recipients. Generalized or widespread vaccinia infection can also occur. Although the heart conditions and vaccinia infection are uncommon, they are potentially deadly.

These risks make sense in the context of smallpox, which is more transmissible and more deadly than monkeypox. ACAM2000 is highly effective in preventing smallpox infection and, if smallpox were to reemerge, the protection would far outweigh the risks of ACAM2000 vaccination. For monkeypox, though, the balance of risks and benefits is less favorable.

If demand for vaccines to fight monkeypox grows beyond the supply of Jynneos, officials may begin to turn to ACAM2000. The recent decision to stretch the supply of Jynneos by allowing the use of lower doses may decrease pressure to use ACAM2000 in the near term, but if the epidemic continues to grow, calls for ACAM2000 use may intensify.

Health departments can now order this vaccine from the Strategic National Stockpile to use in the monkeypox response through an existing Expanded Access Investigational New Drug application, and at least one jurisdiction has already requested this product for potential use against monkeypox.

Although swift and decisive action is imperative to contain the current outbreak, the risks of ACAM2000 require a more deliberative approach. Before making the vaccine more widely available, the FDA should review the available evidence on its safety and effectiveness for preventing monkeypox and present those findings to the Vaccine and Related Biological Products Advisory Committee (VRBPAC). If the FDA and VRBPAC experts recommend the use of ACAM2000, the CDC’s Advisory Committee on Immunization Practices (ACIP) should meet to consider its appropriate use.

Evaluation by these two committees is the standard process for licensing vaccines and recommending them for use in clinical practice. Both committees are staffed by independent experts and the proceedings are open for public viewing and comment. Although it is not required in this instance, leveraging those resources would lend transparency and credibility to a difficult and complex decision.

The monkeypox epidemic is a serious and fast-moving crisis that shows no signs of coming under control. Public health officials should consider all options for protecting people at risk while ending domestic transmission. However, we believe that the risks of ACAM2000 are too serious in this setting to deploy the vaccine without the usual expert review governing the use of new vaccines. Existing review processes at VRBPAC and ACIP can be adapted to ensure that the risks and benefits of ACAM2000 are carefully considered before it is made available to members of the public.

Caitlin Rivers is a senior scholar and epidemiologist at the Johns Hopkins Center for Health Security, and served as the founding associate director of the Center for Forecasting and Outbreak Analytics at the Centers for Disease Control and Prevention. Tom Inglesby is an infectious disease physician, director of the Johns Hopkins Center for Health Security, and a former senior adviser to the Biden administration’s White House Covid-19 Response Team.

3 comments:

Anonymous said...


"BREAKING"
CDC Quietly Removes Statement that Says “mRNA and the Spike Protein Do Not Last Long in the Body” from Their Website.
https://www.thegatewaypundit.com/2022/08/cdc-quietly-removes-statement-says-mrna-spike-protein-not-last-long-body-website/

Should read: CDC admits spike proteins remain in body forever and cause who knows what damage to a person's organs and nervous system. The CDC, Big Pharma, the government and all the people who forced this poison on 3/4 of the population are thanking, whatever God they pray to, that they had the foresight to put immunity deals in place to protect them before jabbing everyone they could with it. "Turning peoples Blood into Pudding, Clots?"

May Fraud cancel out Immunity for these Criminals?

Anonymous said...


**"FLASH-FLASH"**
"German Researchers Examine Covid “Vaccines” and 'Vaccinated People’s Blood' and Say ""Stop Vaccinations"" Immediately"!

The comparison of blood samples from unvaccinated and vaccinated individuals by means of dark-field microscopy showed "noticeable changes in the blood of each person who had been vaccinated with the Covid-19 vaccines". This was evident even if those people hadn’t at that point displayed any visible reaction to the vaccinations. Complex structures similar to those in the vaccines were found in the blood samples of the vaccinated. Using artificial intelligence (AI) image analysis, 'the difference between the blood of vaccinated and unvaccinated people was confirmed.'

https://www.sgtreport.com/2022/08/german-researchers-examine-covid-vaccines-and-vaccinated-peoples-blood-and-say-stop-vaccinations-immediately/

Anonymous said...

Do you think the ACAM2000 could end up starting a smallpox epidemic?

Asking because of this - https://rumble.com/v1gdk8h-if-theyre-using-acam2000-for-monkeypox-that-probably-aint-good....html

(Although I don't take this to be true without more verification, I would love to know what you think.)